Effect of different physiotherapy treatment on low back pain after delivery.

Recruiting

• Conditions: Sacroiliac Joint Dysfunction in Post-Partum Females

• Registration Number: CTRI/2023/08/056798
• Lead Sponsor: Guru Jambheshwar University of Science and Technology

Brief Summary

Sacroiliac joint dysfunction is a very common problem and it is affecting the quality of daily living and has become a serious problem among the post partum females. It can alter the leg length, spinal alignment and affect the quality of daily living. To our knowledge no work has been done to find out the efficacy of therapies focused on SIJD in post partum females. This study will try to provide a effective intervention of SIJD in post partum females. A Randomized controlled trial will be conducted. Initially participants will be screened on the basis of selection criteria. Then they will be randomized into four groups; Mobilizaton group (A), Muscle Energy Technique (B), Core Stabilization exercise group (C), and Control group (D). The participants will be assessed at baseline (Pre intervention data),  and after 6 weeks (post-intervention) and after one month (follow-up) . There will be 18 session in each group (three session per week for 6 weeks). The main objective of the study is to compare the effectiveness of Mobilization, Muscle Energy Technique and Core Stabilisation on SIJD in post partum females.

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2023-08-29
• Study Start: 2023-08-30

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Female
• Target Recruitment: 120

Inclusion Criteria

• 1.Patients with SIJD.
• 2.Primiparous and Multiparous women.

Exclusion Criteria

• Any spine and hip surgery less than 1 year.
• Pregnancy 3.
• Osteoporosis or bone fracture 4.
• Any corticosteroids or anesthetics used for less than 6 months 5.
• Sacroileitis or sacroiliac infection.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Sacral Angle	The participants will be assessed at baseline (Pre intervention data), & after 6 weeks (post-intervention) and after one month (follow-up) . There will be 18 session in each group (three session per week for 6 weeks).
4.Oswestry Disability Index	The participants will be assessed at baseline (Pre intervention data), & after 6 weeks (post-intervention) and after one month (follow-up) . There will be 18 session in each group (three session per week for 6 weeks).
5.EMG	The participants will be assessed at baseline (Pre intervention data), & after 6 weeks (post-intervention) and after one month (follow-up) . There will be 18 session in each group (three session per week for 6 weeks).
2.Photogrammetry	The participants will be assessed at baseline (Pre intervention data), & after 6 weeks (post-intervention) and after one month (follow-up) . There will be 18 session in each group (three session per week for 6 weeks).
3.Gait ( cadence, stride length, step length, walking velocity)	The participants will be assessed at baseline (Pre intervention data), & after 6 weeks (post-intervention) and after one month (follow-up) . There will be 18 session in each group (three session per week for 6 weeks).

Trial Locations

Locations (1)

Guru Jambheshwar University of Science and Technology; 🇮🇳 Hisar, HARYANA, India

Guru Jambheshwar University of Science and Technology

🇮🇳Hisar, HARYANA, India

Pinky

Principal investigator

9996560074

pinkyjangra1992@gmail.com